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. 2015 May 12;17(5):e117. doi: 10.2196/jmir.3717

Table 1.

Demographics and key characteristics at baseline by group (N=49).

Characteristics Experimental group Control group
Caregivers’ characteristics, n 25 24

Caregiver age (years), mean (SD) 64.2 (10.3) 59.0 (12.4)

Female caregiver, n (%) 16 (64) 16 (67)

Children of PWAD,b n (%) 16 (64) 13 (54)

High level of education, n (%) 19 (76) 18 (75)

Middle level of education, n (%) 6 (24) 3 (12)

Living with the PWAD, n (%) 12 (48) 10 (41)

Visiting the PWAD daily, n (%) 4 (16) 2 (8)

Visiting the PWAD at least once per week, n (%) 9 (36) 9 (38)

Psychological/ psychiatric treatment, n (%) 3 (12) 2 (8)

Psychotropic treatment, n (%) 6 (24) 7 (29)

Caregivers with at least another source of stress different to caregiving (eg, work, relationship, family), n (%) 18 (72) 14 (56)

Caregivers with ≥1 professional help,c n (%) 18 (72) 18 (75)

Weekly hours of professional help,d mean (SD) 26.7 (28.7) 8.2 (9.7)

Suffering from a chronic pathology, n (%) 9 (36) 8 (33)
Patients’ characteristics, n 25 24

Onset of symptoms (years), mean (SD), range 4.62 (3.53), 0.55-14.05 4.11 (3), 0.39-12.03

MMSE, mean (SD) 18.5 (5.4) 19.0 (4.6)

IADL scale, mean (SD) 0.6 (0.8) 1.1 (1.1)

a IADL: Instrumental Activities of Daily Living; MMSE: Mini-Mental State Examination; PWAD: persons with Alzheimer’s disease.

b Two participants were not children or spouses (1 daughter-in-law and 1 friend).

c Professional help=housekeeper, nurse, day care, meal delivery.

d Among caregivers receiving respite help.